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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787401Generated: October 29, 2026

Dimethylformamide → 8-Vinyl-1,4-dioxaspiro[4,5]decane

https://huagongshe.com/reaction/1787401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHeptaneHCID 8900—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant8-(2-Iodoethyl)-1,4-dioxaspiro[4.5]decaneHCID 57598630—
SolventWaterHCID 962—
Product8-Vinyl-1,4-dioxaspiro[4,5]decaneHCID 5759891981.5%

Reaction Conditions

Temperature3 °C

Reaction Steps

Fifth Step: 223.0 g of the compound (14) and 800 mL of DMF were added to a reactor under nitrogen atmosphere, and stirred at 3° C. under cooling with ice. 92.9 g of potassium t-butoxide (t-BuOK) was added thereto by dividing into 10 portions at a temperature range of from 3 to 10° C., followed by further stirring at 0° C. for 3 hours. After confirming that the reaction had been completed by GC analysis, the reaction mixture was poured into and mixed with a mixture of 1,500 mL of heptane and 1,500 mL of water at 0° C. The mixture was separated into an organic layer and an aqueous layer by standing still, so as to attain extraction to the organic layer. The resulting organic layer was fractionated and washed with water, followed by drying over anhydrous magnesium sulfate. The resulting organic layer was purified by silica gel column chromatography using heptane as eluent, and the solvent was removed by distillation under reduced pressure. The resulting residue was distilled under reduced pressure to obtain 103.3 g of 8-vinyl-1,4-dioxaspiro[4,5]decane (15) as a colorless transparent liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07510749B2
Source datasetuspto-grants-2009_03
ORD IDord-f75e17883ca9440191277de326bd4422
Source noteuspto-grants-2009_03